Ru/La0.5Pr0.5O1.75 Catalyst for Low-Temperature Ammonia Synthesis

被引:69
作者
Ogura, Yuta [1 ]
Tsujimaru, Kotoko [1 ]
Sato, Katsutoshi [1 ,2 ]
Miyahara, Shin-ichiro [1 ]
Toriyama, Takaaki [3 ]
Yamamoto, Tomokazu [4 ]
Matsumura, Syo [3 ,4 ]
Nagaoka, Katsutoshi [1 ]
机构
[1] Oita Univ, Fac Sci & Technol, Dept Integrated Sci & Technol, 700 Dannoharu, Oita 8701192, Japan
[2] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries, Nishikyo Ku, 1-30 Goryo Ohara, Kyoto 6158245, Japan
[3] Kyushu Univ, Ultramicroscopy Res Ctr, Nishi Ku, Motooka 744, Fukuoka, Fukuoka 8190395, Japan
[4] Kyushu Univ, Dept Appl Quantum Phys & Nucl Engn, Nishi Ku, Motooka 744, Fukuoka, Fukuoka 8190395, Japan
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2018年 / 6卷 / 12期
关键词
NH3; synthesis; Energy carrier; Rare earth oxide; Ru catalyst; Phase change; SUPPORTED RUTHENIUM CATALYSTS; ADSORBED DINITROGEN; HYDROGEN-PRODUCTION; METAL; ACTIVATION; EFFICIENT; ALUMINA; NANOPARTICLES; CHALLENGES; STORAGE;
D O I
10.1021/acssuschemeng.8b04683
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To exploit the use of hydrogen as a source of sustainable energy, development of an efficient process for synthesizing an energy carrier such as ammonia under mild conditions will be necessary. Here, we show that Ru/La0.5Pr0.5O1.75 prereduced at an extraordinary high temperature wof 650 degrees C catalyzes high NH3-synthesis rates under mild conditions. At 400 degrees C under 1.0 MPa, the synthesis rate was comparable with that of most active oxide-supported Ru catalysts. Kinetic analysis revealed that hydrogen poisoning, which is a typical drawback for oxide-supported Ru catalysts such as Cs+/Ru/MgO, was effectively suppressed over Ru/La0.5Pr0.5O1.75. The high activity induced by high-temperature reduction was attributable to the good thermal stability of the support and a phase change of the La0.5Pr0.5O1.75 support during prereduction. Fourier transform-infrared spectroscopy measurements after N-2 adsorption on the catalyst revealed that electrons lwere efficiently donated from trigonal La0.5Pr0.5O1.5 to the antibonding pi orbital of the N N bond of N-2 via Ru atoms. Cleavage of the N N bond, the rate-determining step for ammonia synthesis, was thus accelerated. Our results expand the range of possibilities for developing more effective ammonia synthesis catalysts under mild conditions. Such catalysts will be needed to enable development of hydrogen-based sustainable energy resources.
引用
收藏
页码:17258 / 17266
页数:17
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